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. 2020 Jul 14;8:17. doi: 10.1186/s40170-020-00223-8

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Suppression of ErbB2 breast cancer by MEDICA in vivo. a–c FVB-MMTV-ErbB2 transgenic mice were treated by MEDICA in feed as described in the “Methods” section. *Significant as compared to nontreated. a Breast tumor number (left), weight (middle), and volume (right). Mean (n = 5–6/group). b Tumor ErbB1, ErbB2, phospho-ErbB2(Tyr1248), and ErbB3. Representative blots. c Lung rat ErbB2/neu (V664G) transcript. Mean (n = 9–11/group). d NOD/SCID mice xenografted with RH2111 ErbB2 cells were treated with MEDICA in feed as described in the “Methods” section. Tumor volume (left) and tumor weight (right). Mean ± SD (n = 4–5/group). Significant as compared to nontreated (P < 0.05)